Skip to content
  • Clinical Studies
  • Pharma GMP
  • Pharma Tips
  • Stability Studies
  • Pharma Books
  • Schedule M

SOP Guide for Pharma

The Ultimate Resource for Pharmaceutical SOPs and Best Practices

  • Home
  • Job Safety Analysis (JSA)
    • Oral Dosage Forms (Tablets & Capsules)
    • Oral Liquid Dosage Forms (Syrups, Elixirs, Suspensions, Emulsions)
    • Powder and Granule Dosage Forms
    • Topical Dosage Forms (Creams, Ointments, Gels, Lotions, Pastes)
    • Transdermal Dosage Forms (Patches)
  • Standard Test Procedures (STP)
  • SOP – Blog Post
  • Toggle search form

SOPs for Capsules V 2.0

Capsule: SOP for Cleaning Capsule Shell Manufacturing Machines – V 2.0

Posted on By

The purpose of this SOP is to establish the procedure for cleaning capsule shell manufacturing machines. These machines are responsible for producing the capsule shells used in capsule production. Proper cleaning of these machines is essential to prevent contamination, ensure the quality of the shells, and maintain GMP standards.

Click to read the full article.

Capsules V 2.0

Capsule: SOP for Cleaning Manual Capsule Filling Tools – V 2.0

Posted on By

The purpose of this SOP is to outline the procedure for cleaning manual capsule filling tools. These tools, such as manual capsule fillers, tampers, and capsule trays, are integral to the capsule manufacturing process. Proper cleaning is essential to prevent contamination, maintain GMP standards, and ensure that tools are free from product residues, ensuring the safety and quality of the capsules produced.

Click to read the full article.

Capsules V 2.0

Capsule: SOP for Cleaning Vacuum Systems Used in Capsule Filling – V 2.0

Posted on By

The purpose of this SOP is to outline the cleaning procedure for vacuum systems used in capsule filling. Vacuum systems play a crucial role in maintaining air flow and preventing contamination during capsule manufacturing. Proper cleaning is essential to ensure the system’s functionality, prevent cross-contamination, and ensure that the vacuum system operates within GMP standards.

Click to read the full article.

Capsules V 2.0

Capsule: SOP for Ensuring Cleaning Documentation for Capsule Equipment – V 2.0

Posted on By

The purpose of this SOP is to outline the process for ensuring proper cleaning documentation for capsule manufacturing equipment. It is crucial to maintain accurate and thorough records of all cleaning activities to comply with GMP guidelines, ensure product safety, and guarantee that equipment remains contaminant-free between production cycles. This SOP ensures that all cleaning actions, inspections, and verifications are well-documented for traceability and audit purposes.

Click to read the full article.

Capsules V 2.0

Capsule: SOP for Cleaning Dust Collection Systems in Capsule Production – V 2.0

Posted on By

The purpose of this SOP is to define the procedure for cleaning dust collection systems used in capsule production. These systems are essential for maintaining air quality by capturing dust and particles generated during capsule manufacturing. Regular cleaning ensures the system functions efficiently, prevents cross-contamination, and maintains a safe and clean manufacturing environment.

Click to read the full article.

Capsules V 2.0

Capsule: SOP for Routine Cleaning of Airlocks in Capsule Manufacturing Areas – V 2.0

Posted on By

The purpose of this SOP is to outline the routine cleaning procedure for airlocks in capsule manufacturing areas. Airlocks are critical to maintaining the cleanroom environment by preventing contamination between different areas. Proper cleaning of these airlocks ensures compliance with GMP, reduces the risk of cross-contamination, and maintains product quality.

Click to read the full article.

Capsules V 2.0

Capsule: SOP for Cleaning of Encapsulation Machine Sensors – V 2.0

Posted on By

The purpose of this SOP is to ensure the effective cleaning of sensors used in encapsulation machines. These sensors play a crucial role in the accurate operation of capsule filling machines, and proper cleaning is necessary to avoid inaccuracies caused by dust or product residues. This SOP provides a step-by-step process for cleaning sensors to ensure their optimal performance and longevity.

Click to read the full article.

Capsules V 2.0

Capsule: SOP for Disposal of Cleaning Residues from Capsule Machines – V 2.0

Posted on By

The purpose of this SOP is to define the process for the proper disposal of cleaning residues from capsule manufacturing machines. Proper disposal of residues is critical to avoid contamination, ensure environmental compliance, and maintain workplace safety. This SOP ensures that all residues from cleaning operations, including dust, powders, cleaning agents, and other by-products, are disposed of in accordance with regulatory and safety guidelines.

Click to read the full article.

Capsules V 2.0

Capsule: SOP for Cleaning Blender Machines Used in Capsule Production – V 2.0

Posted on By

The purpose of this SOP is to ensure that blender machines used in the production of capsule formulations are cleaned thoroughly between batches. Effective cleaning is essential to prevent cross-contamination between different capsule formulations and to maintain product quality. This SOP outlines the cleaning process to ensure that blender machines are free from residues, dust, and contaminants before the next production run.

Click to read the full article.

Capsules V 2.0

Capsule: SOP for Cleaning Capsule Size Sorting Machines – V 2.0

Posted on By

The purpose of this SOP is to outline the cleaning procedure for capsule size sorting machines used in capsule manufacturing. Proper cleaning is necessary to maintain the efficiency and accuracy of the size sorting process and to prevent contamination between batches of capsules with different sizes or types. This SOP ensures that the sorting machines are cleaned thoroughly after each production run.

Click to read the full article.

Capsules V 2.0

Posts pagination

Previous 1 … 8 9 10 … 23 Next

Standard Operating Procedures V 1.0

  • Aerosols
  • Analytical Method Development
  • Bioequivalence Bioavailability Study
  • Capsule Formulation
  • Clinical Studies
  • Creams
  • Data Integrity
  • Dental Dosage Forms
  • Drug Discovery
  • Environment, Health and Safety
  • Formulation Development
  • Gels
  • Good Distribution Practice
  • Good Warehousing Practices
  • In-Process Control
  • Injectables
  • Liquid Orals
  • Liposome and Emulsion Formulations
  • Lotions
  • Lyophilized Products
  • Maintenance Dept.
  • Medical Devices
  • Metered-Dose Inhaler
  • Microbiology Testing
  • Nanoparticle Formulation
  • Nasal Spray Formulations
  • Nebulizers
  • Ocular (Eye) Dosage Forms
  • Ointments
  • Otic (Ear) Dosage Forms
  • Pharmacovigilance
  • Powder & Granules
  • Purchase Departments
  • Quality Assurance
  • Quality Control
  • Raw Material Stores
  • Regulatory Affairs
  • Tablet Manufacturing
  • Rectal Dosage Forms
  • Transdermal Patches
  • Vaginal Dosage Forms
  • Validations and Qualifications

Read SOPs in your Language:

 - 
Bengali
 - 
bn
English
 - 
en
Gujarati
 - 
gu
Hindi
 - 
hi
Malayalam
 - 
ml
Marathi
 - 
mr
Punjabi
 - 
pa
Tamil
 - 
ta
Telugu
 - 
te

NEW! Revised SOPs – V 2.0

  • Aerosols V 2.0
  • Analytical Method Development V 2.0
  • API Manufacturing V 2.0
  • BA-BE Studies V 2.0
  • Biosimilars V 2.0
  • Capsules V 2.0
  • Creams V 2.0
  • Elixers V 2.0
  • Ointments V 2.0
  • Raw Material Warehouse V 2.0
  • Tablet Manufacturing V2.0

New Publication: A must for All.

Copyright © 2025 SOP Guide for Pharma.

Powered by PressBook WordPress theme